Thermo Fisher Scientific

ABOUT THERMO FISHER SCIENTIFIC

Thermo Fisher Scientific provides industry-leading pharma services for drug development, clinical trial logistics, and commercial manufacturing. We partner with customers in the pharmaceutical, biotech, and life sciences industries as their trusted CDMO to deliver medicine to patients faster. With more than 60 facilities around the world, we provide end-to-end pharma services across all phases of development and commercial manufacturing, including API, oral solid dose, biologics, cell therapy, mRNA, viral vectors, formulation, clinical trial solutions, logistics services and packaging. We couple our scientific and technical excellence in these areas with a strategic partnership to provide customers of all sizes access to a global network of facilities and dedicated experts across the Americas, Europe, Asia, and Australia. Through our integrated service offerings, we provide tailored solutions to fit your unique drug development journey, accelerating your time to market.

INDUSTRY INSIGHTS

Clinical Trial Logistics: What Biopharma Needs To Prepare For Next

Fragmented clinical trial logistics are slowing programs and increasing risk. Learn how coordinated planning and digital visibility are becoming competitive advantages in complex, global studies.
Clinical Supply Flexibility Where Biotech Programs Need It Most

Flexible clinical development requires scalable infrastructure, strong project management, and global logistics to ensure supply continuity and regulatory compliance.
Packaging And Labeling Support For A Global Cell Therapy Program

Master complex cell therapy logistics with coordinated depots, purpose-built labeling, and temperature-controlled solutions that protect product integrity.
Improving Clinical Trial Label Translation Through Centralized Reuse And Control

Eliminate workflow inefficiencies and regulatory risk in global trials with a centralized translation framework and validated phrase library for consistent, cost-effective execution.
When Every Hour Counts: Emergency Transfer Protects Critical Biomedical Materials

Rapid deployment of specialized cold chain logistics and cryogenic assets ensures strict temperature compliance, protecting critical research continuity and preventing catastrophic material loss.
Flexibility In Drug Development: From Tactical Response To Strategic Discipline

Historically managed through late-stage adjustments, operational adaptability has become a strategic imperative to prevent programs from stalling under real-world pressures.
Optimizing Clinical Supply Management With A One-Team Approach

See how NewAmsterdam Pharma managed 11 global studies across 51 countries and 835 sites for 12,000+ patients without overwhelming their internal team.
Global Trials, Zero Delays: Rethinking Clinical Logistics

This comprehensive guide provides practical insights and best practices for ensuring the timely, secure, and reliable delivery of clinical trial materials worldwide.
Scalable Strategies For Delivering Value In Clinical Trial Logistics

Discover how to transform logistical challenges into strategic advantages with flexible, forward-looking solutions designed for today’s dynamic clinical development landscape.
Delivering Value In Clinical Trial Services By Managing Complexity, Timelines

Gain insights into managing global trial complexity, balancing accelerated timelines with compliance, using advanced technologies to improve efficiency, and leveraging partnerships to support seamless clinical operations.
Navigating Complex Supply Chains: The Critical Role Of UK And EU Qualified Persons

Gain essential insights into QP roles, regulatory updates, and best practices for ensuring compliance, supply continuity, and safe handling of cold and frozen pharmaceutical products across the UK and EU.
How Regional Logistics Strategy Supports Clinical Success In Europe

In an era where trial delays, customs bottlenecks, and fragmented regulations can derail even the most promising program, logistics has become a strategic asset.
Modernizing Clinical Trial Logistics To Deliver Value

Explore how biopharma organizations can design and operate clinical supply systems that absorb complexity while maintaining control and consistency.
Global Reach, Biotech Speed: Clinical Packaging, Labeling That Delivers

By integrating scalable operations, reliable supply chains, and deep regulatory expertise, biotech companies can eliminate bottlenecks, improve efficiency, and accelerate trial execution.

CONTACT INFORMATION

Thermo Fisher Scientific

168 Third Avenue

Waltham, MA 02451

UNITED STATES

Phone: +1 781-622-1000

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PATHEON PHARMA SERVICES SALES INQUIRIES

USA:
+1 919 226-3200

Global:
+1 866 728-4366

SOLUTIONS

Clinical Ancillary Management: Sustainable Services And Products

Reduce lab waste and recover equipment value with our circular and destruction services, including recycling-first disposal, asset redeployment, and pooled supply management.
Accelerating Drug Development Through Integrated CDMO And CRO Partnership

Coordinating drug substance, analytics, and clinical ops across multiple vendors puts you in the integrator role. See how connected CDMO-CRO partnerships eliminate that burden and reduce downstream risk.
Importer Of Record (IOR) Services For Clinical Trials

Global clinical trials face customs challenges. A synchronized Importer of Record service ensures compliance, streamlines logistics, and helps prevent shipment delays.
Destruction And Circular Services

Optimize clinical trial logistics with sustainable lifecycle solutions that reduce waste, lower costs, and maximize laboratory equipment value.
Flexible And Customized Order Solutions For Clinical Ancillary Management

Optimize global clinical trial logistics with scalable ancillary supply management, from cost-effective shipping to complex kitting and expiry control.
Distribution Automation System For Clinical Supply Chains

Automated storage and retrieval technology reduces mis-picks, speeds order processing, and keeps clinical trial materials moving on time as study demands shift.
Accelerate Drug Development With Innovative 360˚ CDMO And CRO Solutions

Accelerator™ Drug Development provides a strategic, end-to-end partnership model that helps sponsors optimize resources, overcome development challenges, and advance promising therapies.
Designing Clinical Packaging For A New Era Of Trial Complexity

See how innovative packaging engineering approaches are helping study teams adapt to evolving clinical trial requirements with greater speed and flexibility.
How To Advance Self-Administered Therapies

Scale your biologic fill-finish from vials to autoinjectors without disruption. See how integrated device assembly capabilities support every clinical phase through commercialization.
The Shift Toward Self-Administration And Integrated Supply Chains

Adopt integrated, end-to-end clinical supply strategies that enable self-administered therapies, reduce patient burden, and accelerate clinical trial timelines while improving access and outcomes.
Autoinjector, Pen, And Prefilled Syringe Capabilities

Flexible, scalable capabilities for autoinjectors, pens, and prefilled syringes — ranging from manual to fully automated — streamlining and simplifying your biologic drug development supply chain.
Accelerator™ Drug Development 360° CDMO And CRO Solutions

Review this coordinated suite of integrated solutions that brings together CDMO and CRO capabilities across clinical research, manufacturing, and clinical supply.
ATLAS Label Translation Solution

By simplifying label requests, integrating expert translation and regulatory support, and enabling a fully paperless approval workflow, organizations can reduce turnaround times while maintaining high-quality label content.
Biorepository And Lab Services

Beyond basic storage, our comprehensive services deliver fully compliant, state-of-the-art environments where samples are meticulously cataloged, tracked, and maintained with precision.